510(k) K011102 ยท HWC Screw, Fixation, Bone
ANTERIOR CRUCIATE LIGAMENT (ACL) INSTRUMENT SYSTEM
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Aug 3, 2001 |
| Received | Apr 11, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011102
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.